O'Neill R E, Palese P
Department of Microbiology, Mount Sinai School of Medicine, New York, New York 10029.
Infect Agents Dis. 1994 Apr-Jun;3(2-3):77-84.
Influenza A virus RNA replication and expression is directed from cis-acting sequences present on the viral RNAs with the help of trans-acting factors encoded by the virus. Ribonucleoprotein (RNP) complexes reconstituted from synthetic cDNA-derived RNA and purified viral proteins have facilitated the dissection of these cis-acting signals and trans-acting factors. Prior to these studies influenza viruses and other negative-strand RNA viruses were refractory to molecular genetic manipulations. These reverse genetic studies have helped in defining the promoter and polyadenylation signals required for viral RNA synthesis. Studies involving the use of reconstituted RNP complexes have revealed that the viral proteins PB1, PB2, PA, and the nucleoprotein (NP) are necessary for replication and expression of influenza virus RNA. Inroads have also been made in determining the cellular proteins that participate in influenza virus gene expression and replication. The yeast interactive trap system has been used to identify and clone a gene (NPI-1), which encodes a protein that interacts with the influenza virus NP suggesting that this cellular protein is a trans-acting factor functioning in viral RNA synthesis.
甲型流感病毒RNA的复制和表达由病毒RNA上存在的顺式作用序列在病毒编码的反式作用因子的帮助下进行指导。从合成的cDNA衍生RNA和纯化的病毒蛋白重构的核糖核蛋白(RNP)复合物有助于剖析这些顺式作用信号和反式作用因子。在这些研究之前,流感病毒和其他负链RNA病毒对分子遗传学操作具有抗性。这些反向遗传学研究有助于确定病毒RNA合成所需的启动子和聚腺苷酸化信号。涉及使用重构RNP复合物的研究表明,病毒蛋白PB1、PB2、PA和核蛋白(NP)对于流感病毒RNA的复制和表达是必需的。在确定参与流感病毒基因表达和复制的细胞蛋白方面也取得了进展。酵母相互作用陷阱系统已被用于鉴定和克隆一个基因(NPI-1),该基因编码一种与流感病毒NP相互作用的蛋白,表明这种细胞蛋白是在病毒RNA合成中起作用的反式作用因子。